Disease-causing R1185C mutation of WNK4 disrupts a regulatory mechanism involving calmodulin binding and SGK1 phosphorylation sites. [electronic resource]
Producer: 20130403Description: F8-F18 p. digitalISSN:- 1522-1466
- Animals
- Binding Sites -- physiology
- Calcium -- pharmacology
- Calmodulin -- metabolism
- Humans
- Immediate-Early Proteins -- metabolism
- Oocytes -- metabolism
- Phosphorylation
- Protein Serine-Threonine Kinases -- genetics
- Pseudohypoaldosteronism -- genetics
- Sodium-Potassium-Chloride Symporters -- metabolism
- Solute Carrier Family 12, Member 1
- Xenopus laevis
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Publication Type: Journal Article; Research Support, N.I.H., Extramural
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